Variant report

Variant	rs4672158
Chromosome Location	chr2:56957466-56957467
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs1016409	0.81[AFR][1000 genomes]
rs10174159	0.85[ASN][1000 genomes]
rs10174228	0.85[ASN][1000 genomes]
rs10175703	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10175921	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10177812	0.85[ASN][1000 genomes]
rs10182642	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10183578	0.92[ASN][1000 genomes]
rs10193478	0.86[EUR][1000 genomes]
rs10194864	0.86[EUR][1000 genomes]
rs10200459	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs10202272	0.86[EUR][1000 genomes]
rs10208734	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10210024	0.86[AFR][1000 genomes]
rs11125648	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11125659	0.86[EUR][1000 genomes]
rs11885280	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11885371	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11889432	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11889483	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11893528	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11894249	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11895018	0.86[EUR][1000 genomes]
rs11897725	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11900216	0.86[EUR][1000 genomes]
rs11902041	1.00[EUR][1000 genomes]
rs12105442	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12465575	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12470816	0.81[AMR][1000 genomes]
rs12472267	0.86[EUR][1000 genomes]
rs12477721	0.86[EUR][1000 genomes]
rs13387012	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13387189	0.87[EUR][1000 genomes]
rs13400486	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13411712	0.86[EUR][1000 genomes]
rs13415063	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13419971	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13423875	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17048395	0.86[EUR][1000 genomes]
rs1996704	0.86[EUR][1000 genomes]
rs2161028	0.96[ASN][1000 genomes]
rs2682839	0.84[AFR][1000 genomes]
rs28501480	0.86[EUR][1000 genomes]
rs28591144	0.86[EUR][1000 genomes]
rs28604555	1.00[EUR][1000 genomes]
rs28682440	0.86[EUR][1000 genomes]
rs2870074	0.85[ASN][1000 genomes]
rs2870076	0.85[ASN][1000 genomes]
rs4671294	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4671295	0.86[AFR][1000 genomes]
rs4672146	0.86[EUR][1000 genomes]
rs4672147	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4672148	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4672151	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4672155	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4672156	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4672157	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60798964	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61553870	0.85[ASN][1000 genomes]
rs6713552	0.85[ASN][1000 genomes]
rs6713559	0.85[ASN][1000 genomes]
rs6729559	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6730067	0.94[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6732353	0.85[ASN][1000 genomes]
rs6742211	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6758203	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73940764	0.88[AMR][1000 genomes]
rs7572849	0.86[EUR][1000 genomes]
rs7574093	0.85[ASN][1000 genomes]
rs7577678	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7583523	0.86[EUR][1000 genomes]
rs7585003	0.85[ASN][1000 genomes]
rs977388	0.85[ASN][1000 genomes]
rs978566	0.85[AFR][1000 genomes]
rs9808420	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008859	chr2:56767452-57126026	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv535726	chr2:56767452-57126026	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv874179	chr2:56817927-56957466	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv874180	chr2:56822558-56957466	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv582058	chr2:56892585-57016392	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv582059	chr2:56892585-57175087	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv535727	chr2:56895497-57059359	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv1007347	chr2:56904928-57100439	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv582060	chr2:56941668-57137622	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:56957000-56958600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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